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2-Bromo-5-fluorobenzaldehyde

CAS No.
94569-84-3
Chemical Name:
2-Bromo-5-fluorobenzaldehyde
Synonyms
2-BROMO-5-FLUOROBENZALDHYDE;2-bromo-5-fluorobenzaldehydy;2-BROMO-5-FLUOROBENZALDEHYDE;5-Fluoro-2-Bromo benzaldehyde;Benzaldehyde, 2-broMo-5-fluoro-;2-Bromo-5-fluorobenzaldehyde 96%;2-Bromo-5-fluorobenzaldehyde >2-Bromo-5-fluorobenzaldehyde ,98%;2-BroMo-5-fluorobenzaldehyde, 95+%;2-Bromo-5-fluorobenzaldehyde ISO 9001:2015 REACH
CBNumber:
CB0147156
Molecular Formula:
C7H4BrFO
Molecular Weight:
203.01
MDL Number:
MFCD00142872
MOL File:
94569-84-3.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:53

2-Bromo-5-fluorobenzaldehyde Properties

Melting point 51-56 °C (lit.)
Boiling point 225.8±20.0 °C(Predicted)
Density 1.670±0.06 g/cm3(Predicted)
Flash point 190 °F
storage temp. 2-8°C
solubility Soluble in methanol.
form powder to lump
color White to Orange to Green
Sensitive Air Sensitive
InChI InChI=1S/C7H4BrFO/c8-7-2-1-6(9)3-5(7)4-10/h1-4H
InChIKey CJUCIKJLMFVWIS-UHFFFAOYSA-N
SMILES C(=O)C1=CC(F)=CC=C1Br
CAS DataBase Reference 94569-84-3(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37/39-24/25
WGK Germany  3
Hazard Note  Irritant
HS Code  29130000
NFPA 704
2
2 1

2-Bromo-5-fluorobenzaldehyde price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 528978 2-Bromo-5-fluorobenzaldehyde 96% 94569-84-3 5g $98.3 2024-03-01 Buy
Sigma-Aldrich 528978 2-Bromo-5-fluorobenzaldehyde 96% 94569-84-3 1g $30.4 2023-06-20 Buy
TCI Chemical B2353 2-Bromo-5-fluorobenzaldehyde >95.0%(GC) 94569-84-3 5g $56 2024-03-01 Buy
TCI Chemical B2353 2-Bromo-5-fluorobenzaldehyde >95.0%(GC) 94569-84-3 25g $166 2024-03-01 Buy
Alfa Aesar B25071 2-Bromo-5-fluorobenzaldehyde, 98% 94569-84-3 5g $61.65 2024-03-01 Buy
Product number Packaging Price Buy
528978 5g $98.3 Buy
528978 1g $30.4 Buy
B2353 5g $56 Buy
B2353 25g $166 Buy
B25071 5g $61.65 Buy

2-Bromo-5-fluorobenzaldehyde Chemical Properties,Uses,Production

Chemical Properties

White to light yellow solid

Uses

2-Bromo-5-fluorobenzaldehyde may be used in the synthesis of dihydrobenzoxaboroles bearing aryl, heteroaryl or vinyl substituents at the 1-position and 5-fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole.

Uses

2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting , dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N'-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction.

General Description

2-Bromo-5-fluorobenzaldehyde can be prepared by reacting 2-bromo-5-fluorotoluene with N-bromosuccinimide. Its crystals exhibit monoclinic crystal system and space group P21/c.

Synthesis

2-Bromo-5-fluorobenzyl alcohol

202865-66-5

2-Bromo-5-fluorobenzaldehyde

94569-84-3

General procedure for the synthesis of 2-bromo-5-fluorobenzaldehyde from 2-bromo-5-fluorobenzyl alcohol: to a solution of 2-bromo-5-fluorobenzyl alcohol (0.852 g, 4.156 mmol) in dichloromethane (15 mL) was added manganese dioxide (4.254 g, 85%, 41.56 mmol). The reaction mixture was stirred at room temperature for 48 h. The solid was subsequently separated by filtration and washed with dichloromethane. The filtrate was concentrated to give 777 mg of 2-bromo-5-fluorobenzaldehyde (92% yield). Subsequently, the newly prepared 2-bromo-5-fluorobenzaldehyde (0.777 g, 3.828 mmol) was dissolved in anhydrous tetrahydrofuran (10 mL) and the solution was cooled to 0 °C. At low temperature, trifluoromethyltrimethylsilane (1.13 mL, 7.656 mmol) and tetrabutylammonium fluoride (0.020 g, 0.076 mmol) were added sequentially. After that, the reaction mixture was slowly warmed up to room temperature and stirring was continued at that temperature for 5 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate, washed sequentially with water and brine and dried with magnesium sulfate. The solvent was removed under reduced pressure to afford 1.1 g (90% purity) of the crude product of 2-bromo-5-fluorophenyl-2,2,2-trifluoroethanol, which could be used in subsequent steps without further purification.

References

[1] New Journal of Chemistry, 2017, vol. 41, # 22, p. 13377 - 13381
[2] Patent: US2008/153852, 2008, A1. Location in patent: Page/Page column 23
[3] RSC Advances, 2014, vol. 4, # 25, p. 12834 - 12839
[4] Tetrahedron, 2015, vol. 71, # 38, p. 6744 - 6748
[5] Patent: CN104817441, 2017, B. Location in patent: Paragraph 0050-00053

202865-66-5
94569-84-3
Synthesis of 2-Bromo-5-fluorobenzaldehyde from 2-Bromo-5-fluorobenzyl alcohol
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View Lastest Price from 2-Bromo-5-fluorobenzaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Bromo-5-fluorobenzaldehyde pictures 2025-07-07 2-Bromo-5-fluorobenzaldehyde
94569-84-3
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mujin Biotechnology Co.,Ltd
2-Bromo-5-fluorobenzaldehyde pictures 2025-06-24 2-Bromo-5-fluorobenzaldehyde
94569-84-3
US $0.00-0.00 / KG 1KG 99% 20 mt Hebei Chuanghai Biotechnology Co., Ltd
2-Bromo-5-fluorobenzaldehyde pictures 2025-05-26 2-Bromo-5-fluorobenzaldehyde
94569-84-3
US $10.00 / KG 1KG 99.% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
2-Bromo-5-fluorobenzaldehyde 96% 2-BROMO-5-FLUOROBENZALDEHYDE 5-Fluoro-2-Bromo benzaldehyde 2-BROMO-5-FLUOROBENZALDHYDE 2-Bromo-5-fluorobenzaldehyde ,98% 2-BroMo-5-fluorobenzaldehyde, 95+% Benzaldehyde, 2-broMo-5-fluoro- 2-Bromo-5-fluorobenzaldehyde > 2-Bromo-5-fluorobenzaldehyde ISO 9001:2015 REACH 2-bromo-5-fluorobenzaldehydy 94569-84-3 BrC6H4FCHO C7 Carbonyl Compounds Aldehydes Building Blocks Organic Building Blocks Ipragliflozin Aryl Fluorinated Building Blocks Building Blocks Chemical Synthesis Fluorinated Building Blocks Organic Building Blocks Organic Fluorinated Building Blocks Other Fluorinated Organic Building Blocks Aromatic Aldehydes & Derivatives (substituted) Furans, Benzofurans & Dihydrobenzofurans Phenyls & Phenyl-Het Benzaldehyde API intermediates Benzaldehyde series Aldehydes blocks FluoroCompounds Carbonyl Compounds Adehydes, Acetals & Ketones Bromine Compounds Fluorine Compounds Phenyls & Phenyl-Het Furans, Benzofurans & Dihydrobenzofurans C7 Carbonyl Compounds